HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800426Generated: November 1, 2026
Potassium Carbonate → Tert-butyl 2-(4-methylpiperazin-1-yl)acetate
https://huagongshe.com/reaction/1800426
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | tert-Butyl chloroacetate | HCID 66052 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Tert-butyl 2-(4-methylpiperazin-1-yl)acetate | HCID 11816730 | 79.1% |
Reaction Steps
To a suspension of tert-butyl chloroacetate (3.49 g, 34.9 mmol) and potassium carbonate (5.50 g, 39.8 mmol) in acetonitrile (300 mL) was added dropwise 1-methylpiperazine (5.00 g, 33.2 mmol), and the mixture was stirred with heating at 50° C. for 16 hr. The reaction mixture was cooled to room temperature, the insoluble material was filtered off, and the filtrate was concentrated. Water (150 mL) was added to the obtained residue, and the mixture was extracted with ethyl acetate (300 mL). The organic layer was washed with water (150 mL) and saturated brine (150 mL), and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated to give the title compound (5.63 g, 79%) as a pale-yellow oil. The compound was used for the next reaction without further purification operation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344135B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-bba6cf0298974c64a9d7f130f8cdf563 |
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| Source note | uspto-grants-2013_01 |
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